Evidence map›Paper›PMID 41037805›Full record

ArticleJMIR research protocols2025

Identifying Optimal Testing Modalities to Increase COVID-19 Testing Access in Baltimore, Maryland: Protocol for a Household Randomized Controlled Trial.

Jessica Duchen, Alexandra K Mueller, Saifuddin Ahmed, Jamie Perin, Courtney Borsuk, Joshua Trowell, Kelly Lowensen, Steven Huettner, Andy Peytchev, Jason E Farley and 2 more

Abstract read
In one paragraph

Article in JMIR research protocols, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jessica DuchenCenter for Child and Community Research, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, United States.ORCID 0000-0003-0756-3474
Alexandra K MuellerCenter for Child and Community Research, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, United States.ORCID 0000-0003-1130-6251
Saifuddin AhmedDepartment of Population, Family and Reproductive Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.ORCID 0000-0002-9884-4580
Jamie PerinCenter for Child and Community Research, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, United States.ORCID 0000-0002-5482-6620
Courtney BorsukDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.ORCID 0000-0003-3429-2745
Joshua TrowellDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.ORCID 0000-0003-4311-4609
Kelly LowensenCenter for Infectious Disease and Nursing Innovation, Johns Hopkins School of Nursing, Baltimore, MD, United States.ORCID 0009-0000-1022-4241
Steven HuettnerCenter for Child and Community Research, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, United States.ORCID 0000-0003-4904-1455
Andy PeytchevCenter for Survey Methodology, Survey Research Division, Research Triangle Institute International, Research Triangle Park, NC, United States.ORCID 0000-0002-6886-9867
Jason E Farley *Center for Infectious Disease and Nursing Innovation, Johns Hopkins School of Nursing, Baltimore, MD, United States.ORCID 0000-0002-6896-0134
Shruti H Mehta *Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.ORCID 0000-0002-2523-0959
Jacky M Jennings *Center for Child and Community Research, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, United States.ORCID 0000-0002-3789-5122

Funding

Vaccine Response and Immunotherapeutics SWGP30AI094189 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Richard E. Chaisson · 2012 to 2026
$67.0M
NIAID NIH HHS P30 AI094189
6 · The paper itself

Abstract

backgroundThe COVID-19 pandemic disproportionately affected low-income and racial and ethnic minority populations. Testing plays a critical role in disrupting disease transmission, but complex barriers prevent optimal testing access, particularly for Black and Latinx communities. There is limited evidence regarding the optimal testing modalities to increase testing access for these populations.

objectiveThis study aimed to define the optimal COVID-19 testing modalities for maximizing testing acceptance, uptake, and timeliness of receipt of results.

methodsThe Community Collaboration to Combat COVID-19 (C-FORWARD) trial was a household randomized comparative effectiveness trial conducted in a representative sample of an urban population. Households across 653 census block groups were sampled using a probability proportional to size approach. The primary outcome was the completion of SARS-CoV-2 or COVID-19 testing within 30 days of randomization.

resultsBetween February 2021 and December 2022, a total of 1083 individuals were enrolled, including 881 (81.35%) index participants and 202 (18.65%) household members. The mean age of participants was 51 (SD 18) years.Of the total sample, 43% (n=460) of participants identified as Black or African American, 48.6% (n=526) as White, and 9% (n=91) as other, including Asian, American Indian, Native Hawaiian or Pacific Islander, and multiple races; 4.8% (n=48) of participants identified as Hispanic or Latino. At the time of enrollment, 51.1% (n=553) were currently working either full time or part time, and 32.9% (n=342) of participants had an advanced degree. In total, 80% (n=809) of participants had been tested for COVID-19 previously, with 22.3% (n=179) reporting a prior positive test for COVID-19, and 86.8% (n=890) reporting receiving at least one COVID-19 vaccination before enrollment.

conclusionsData from the C-FORWARD trial will be used to address important questions regarding COVID-19 testing acceptance and uptake in an urban population. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR1-10.2196/68600.

Indexed as

COVID-19COVID-19 TestingHealth Services AccessibilityAdultBaltimoreFamily CharacteristicsFemaleHumansMaleMiddle AgedPatient Acceptance of Health CareRandomized Controlled Trials as TopicSARS-CoV-2disease controlhealthcare accesshealth disparitieshealth equityinfectious diseasemobileSARS-CoV-2urban health

Identifiers

PMID41037805
PMCPMC12531582

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.